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  • motor agraphia
    ¿îµ¿¾²±â¾ð¾îºÒ´É(Áõ), ¿îµ¿½Ç¼­Áõ
  • motor alexia
    ¿îµ¿Àбâ¾ð¾î»ó½Ç(Áõ), ¿îµ¿½Çµ¶Áõ
  • motor aphasia
    ¿îµ¿¾ð¾î»ó½ÇÁõ, ¿îµ¿½Ç¾îÁõ
  • motor apraxia
    ¿îµ¿ÇàÀ§»ó½Ç(Áõ), ¼÷·ÃÇàÀ§»ó½Ç(Áõ), ¿îµ¿½ÇÇàÁõ
  • motor area
    ¿îµ¿¿µ¿ª
  • motor aura
    ¿îµ¿Á¶Áü
  • motor behavior
    ¿îµ¿ÇàÀ§
  • motor cell
    ¿îµ¿½Å°æ¼¼Æ÷
  • motor cilium
    ¿îµ¿¼¶¸ð
  • motor cortex
    ¿îµ¿°ÑÁú, ¿îµ¿ÇÇÁú
  • motor end organ
    ¿îµ¿Á¾¸»±â°ü
  • motor endplate
    ¿îµ¿Á¾¸»ÆÇ
  • motor evoked potential
    ¿îµ¿À¯¹ßÀüÀ§
  • motor fiber
    ¿îµ¿¼¶À¯, ¿îµ¿½Å°æ¼¶À¯
  • motor fitness
    ¿îµ¿ÀûÇÕ¼º
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  • ¿µ¹®
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  • motor agraphia
    ¿îµ¿¾²±â¾ð¾î»ó½ÇÁõ
  • motor alexia
    ¿îµ¿¼ºÀбâ¾ð¾î»ó½ÇÁõ
  • motor amimia
    ¿îµ¿Ç¥Á¤¾ð¾î»ó½ÇÁõ
  • motor amusia
    ¿îµ¿À½Ä¡Áõ
  • motor aphasia
    ¿îµ¿¾ð¾î»ó½ÇÁõ
  • motor apraxia
    ¿îµ¿ÇàÀ§»ó½ÇÁõ, ¼÷·ÃÇàÀ§»ó½ÇÁõ
  • motor area
    ¿îµ¿¿µ¿ª
  • motor aura
    ¿îµ¿Á¶Áü
  • motor speech area
    ¿îµ¿¾ð¾î±¸¿ª
  • somatic motor aura
    ¸ö¿îµ¿Á¶Áü
  • supplemental motor area
    º¸Á¶¿îµ¿±¸¿ª
  • motor behavior
    ¿îµ¿ÇàÀ§
  • motor paralytic neurogenic bladder
    ½Å°æÅ¿¿îµ¿¸¶ºñ¹æ±¤
  • motor cell
    ¿îµ¿½Å°æ¼¼Æ÷
  • motor cilium
    ¿îµ¿¼¶¸ð
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  • partial saturation spin echo sequence
    ºÎºÐ Æ÷È­ ½ºÇÉ ¿¡ÄÚ ¿¬¼â
  • partial saturation state
    ºÎºÐ Æ÷È­ »óÅÂ
  • partial sequence
    ºÎºÐ¼­¿­.
  • partial sex linkage
    ºÎºÐ¹Ý¼º(¡­Úãàõ).
  • partial sex linkage inheritance
    ºÎºÐÀû ¹Ý¼ºÀ¯Àü.
  • partial shell crown
    ±¹ºÎ±Ý°ü.
  • partial splenic arterial embolization
    ºÎºÐÀû ºñµ¿¸Æ »öÀü¼ú
  • partial stapedectomy
    µî°ñºÎºÐÀýÁ¦¼ú
  • partial thickness graft
    ºÎºÐÃþÀ̽Ä(Æí)
  • partial thromboplastin time =PTT
    ºÎºÐÆ®·Òº¸ÇÃ¶ó½ºÆ¾½Ã°£.
  • partial thromboplastin time=PTT
    ºÎºÐÆ®·Òº¸ÇÃ¶ó½ºÆ¾½Ã°£
  • partial thyroidectomy
    °©»ó¼±ºÎºÐÀýÁ¦¼ú.
  • partial tolerance
    ºÎºÐ°ßµõ
  • partial tone
    ºÎºÐÀ½
  • partial transposition
    ºÎºÐÀû Ç÷°üÀüÀ§(Ý»ÝÂîÜúìηï®êÈ).
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MERRF myoclonus epilepsy with ragged red fibers [syndrome]
MERRLA myoclonus epilepsy-ragged red fibers-lactic acidosis [syndrome]
NASE National Association for the Study of Epilepsy
NCE negative contrast echocardiography; new chemical entity; nonconvulsive epilepsy
PME periodic monitoring examination; phosphomonoester; polymorphonuclear eosinophil; progressive myoclon...
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MERRF myoclonus epilepsy and ragged red fiber
APTT Activated Partial Thromboplastin Time
APTT Activated partial thromboplastin
APOLT Auxiliary partial orthotopic liver transplantation
CPS Complex partial seizure
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  • motor oculi
    µ¿¾È ½Å°æ
  • motor output disorder
    ¿îµ¿¼º Ãâ·Â Àå¾Ö
  • motor paralytic neurogenic bladder
    ¿îµ¿ ¸¶ºñ¼º ½Å°æÀμº ¹æ±¤
  • motor perceptor
    ¿îµ¿ ÀνÄ
  • motor point
    ¿îµ¿ Á¡
  • motor reflex
    ¿îµ¿ ¹Ý»ç
    ¿îµ¿ ±â±¸ ¸»Ãʸ¦ ÀÚ±ØÇÔÀ¸·Î½á ÀϾ´Â ¹Ý»ç.
  • motor responsiveness
    ¿îµ¿ ¹ÝÀÀ¼º
  • motor seizure
    ¿îµ¿ ¹ßÀÛ
  • motor skills disorder
    ¿îµ¿ ´É·Â Àå¾Ö
  • motor speech center
    ¿îµ¿¼º ¾ð¾î ÁßÃß
  • motor syndrome
    ¿îµ¿ ÁßÃß ÁõÈıº
  • motor system disease
    ¿îµ¿°è Àå¾Ö
  • motor tract
    ¿îµ¿·Î
  • motor wave
    ¿îµ¿ÆÄ
  • motor zone
    ¿îµ¿´ë
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cortical epilepsy Epilepsy of various aetiologies characterised by focal seizures or secondarily generalised tonic-clonic seizures. Ictal symptoms are often related to the brain region where the seizure begins focally.
Synonym: cortical epilepsy, local epilepsy, partial epilepsy.
(05 Mar 2000)
myoclonic astatic epilepsy A petit mal variant characterised by atonic (drop attacks) and tonic or tonic-clonic attacks in neurologically disabled (hemiplegic, ataxic, etc.) children with mental retardation; characterised in EEG by 2/sec spike and wave discharges; usually progresses in spite of medication.
(05 Mar 2000)
myoclonus epilepsy A clinically diverse group of epilepsy syndromes, some benign, some progressive. Many are hereditary with mendelian and nonmendelian mitochondrial inheritance. All are characterised by the occurrence of myoclonus, which may be limited or predominate in the condition. Specific syndromes include cherry red spot myoclonus syndrome, ceroid lipofuscinosis, myoclonic epilepsy with ragged red fibres, and Baltic myoclonus.
Synonym: localization related epilepsy.
(05 Mar 2000)
cryptogenic epilepsy tonic-clonic seizure
posttraumatic epilepsy A convulsive state following and causally related to head injury; with brain damage either manifested clinically or ascertained by special examinations such as computed tomography. To assume causal relationship, the individual must have had no previous epilepsy, no cerebral disease, and no other brain trauma. The attacks should have started, depending on the severity of the wounding, within 3 months to 2 years of the alleged trauma and be of a type compatible with the site of injury and the EEG abnormalities.
(05 Mar 2000)
primary generalised epilepsy Epilepsy without evidence of focal or multifocal central nervous system disease. Seizures are generalised from onset, both by EEG and clinical criteria. Often a pure genetic form of epilepsy.
See: generalised tonic-clonic seizure.
(05 Mar 2000)
procursive epilepsy A psychomotor attack initiated by whirling or running.
(05 Mar 2000)
psychomotor epilepsy Attacks with elaborate and multiple sensory, motor, and/or psychic components, the common feature being a clouding or loss of consciousness and amnesia for the event; clinical manifestations may take the form of automatisms; emotional outbursts of temper, anger or show of fear; motor or psychic disturbances; or may be related to any sphere of human activity. Electroencephalographically, the attack is characterised by spike discharges in the temporal lobe, especially in sleep.
See: procursive epilepsy, visceral epilepsy, uncinate epilepsy.
Synonym: automatic epilepsy, psychomotor seizure.
(05 Mar 2000)
secondary generalised epilepsy A group of epilepsy syndromes of diverse aetiologies with diffuse or multifocal cerebral involvement. Patients typically have a variety of generalised seizure types, including tonic, atonic, myoclonic, atypical absence, and generalised tonic-clonic seizures. Partial seizures may also occur. One classic syndrome is the Lennox-Gastaut syndrome.
Synonym: symptomatic epilepsy.
(05 Mar 2000)
sensory epilepsy Focal epilepsy initiated by a somatosensory phenomenon.
(05 Mar 2000)
sensory precipitated epilepsy Seizures which are induced by peripheral stimulation; e.g., audiogenic, laryngeal, photogenic, or other stimulation.
Synonym: sensory precipitated epilepsy.
(05 Mar 2000)
sleep epilepsy Incorrect term for narcolepsy.
(05 Mar 2000)
somnambulic epilepsy Postictal automatism in which the patient walks or runs about exhibiting natural behaviour of which he or she has no subsequent remembrance.
(05 Mar 2000)
startle epilepsy A form of reflex epilepsy precipitated by sudden noises.
(05 Mar 2000)
nocturnal epilepsy An epilepsy syndrome characterised by nocturnal seizures only.
(05 Mar 2000)
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